Gene Expression Literature Summary

• Symbol: Mns1
• Name: meiosis-specific nuclear structural protein 1
• ID: MGI:107933

6 matching records from 6 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E8	E8.5	E12.5	E14.5	E15	E15.5	E16	P
Immunohistochemistry (section)	1							1
In situ RNA (section)				1		1
In situ RNA (whole mount)		1
RT-PCR			1		1		1	1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Mns1  meiosis-specific nuclear structural protein 1
Results	Reference
1*	J:313619 Bedogni F, Hevner RF, Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development. Front Mol Neurosci. 2021;14:686034
3*	J:46439 Freeman TC, Dixon AK, Campbell EA, Tait TM, Richardson PJ, Rice KM, Maslen GL, Metcalfe AD, Streuli CH, Bentley DR, Expression Mapping of Mouse Genes. MGI Direct Data Submission. 1998;
2	J:353048 Lu H, Twan WK, Ikawa Y, Khare V, Mukherjee I, Schou KB, Chua KX, Aqasha A, Chakrabarti S, Hamada H, Roy S, Localisation and function of key axonemal microtubule inner proteins and dynein docking complex members reveal extensive diversity among vertebrate motile cilia. Development. 2024 Jul 15;151(14):dev202737
1	J:86350 Schwab K, Patterson LT, Aronow BJ, Luckas R, Liang HC, Potter SS, A catalogue of gene expression in the developing kidney. Kidney Int. 2003 Nov;64(5):1588-604
1	J:294106 Soulez M, Saba-El-Leil MK, Turgeon B, Mathien S, Coulombe P, Klinger S, Rousseau J, Levesque K, Meloche S, Reevaluation of the Role of Extracellular Signal-Regulated Kinase 3 in Perinatal Survival and Postnatal Growth Using New Genetically Engineered Mouse Models. Mol Cell Biol. 2019 Mar 15;39(6)
1*	J:265340 Ta-Shma A, Hjeij R, Perles Z, Dougherty GW, Abu Zahira I, Letteboer SJF, Antony D, Darwish A, Mans DA, Spittler S, Edelbusch C, Cindric S, Nothe-Menchen T, Olbrich H, Stuhlmann F, Aprea I, Pennekamp P, Loges NT, Breuer O, Shaag A, Rein AJJT, Gulec EY, Gezdirici A, Abitbul R, Elias N, Amirav I, Schmidts M, Roepman R, Elpeleg O, Omran H, Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility. PLoS Genet. 2018 Aug;14(8):e1007602